Category: Amyotrophic Lateral Sclerosis

The “Ice Bucket Challenge” has made the rare disease “cryonic man” no longer unheard of by the public. The media coverage of the “frozen people” is also a sad piece…

Amyotrophic lateral bundle sclerosis is the most common type of motor neuron disease, selectively damaging the anterior horn of the spinal cord and the motor nerve nuclei of the brainstem,…

Amyotrophic lateral sclerosis is a hereditary disease that is directly inherited in a small percentage of families. If it is some adult onset amyotrophic lateral sclerosis patients, it is found…

Tests required for the diagnosis of ALS/MND Blood chemistry tests include sedimentation, C-reactive protein, routine blood tests, transaminases and lactate dehydrogenase, thyroid function, vitamin B12 and folate, serum protein electrophoresis,…

　　The use of mainly sweet medicine into the tea or into the meal, in the four seasons of prevention, treatment of minor illnesses, serious aids and post-illness conditioning, etc. all…

　　At present, there is no effective treatment for this disease, and the main treatments are as follows.　　1. Riluzole may delay the onset of respiratory dysfunction and prolong survival in ALS…

　　First of all, for adults, amyotrophic lateral sclerosis is often seen in men under 50 years of age with the disease most often the symptoms of the cause of the…

　　Muscle MRI is one of the five major adjuvant examinations for muscle disease and has a history of 20 years of clinical development. The study of muscle MRI was first…

　　A new study suggests that foods rich in omega-3 polyunsaturated fatty acids (PUFA) may help reduce the risk of amyotrophic lateral sclerosis (ALS).　　The study, published in JAMA Neurology on July…

　　1. exertional spirometry (FVC) values.　　FVC is the most important predictor of survival; Fallat found that FVC